rs1310173085
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
2
Location
8733542
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.3955T>C (p.Ser1319Pro)
Allele
G
Clinical Significance
Uncertain significance